Chrystelle Colas

17PUBLICATIONS
84CO-AUTHORS
Microelectromechanical systems (MEMS)Nutritional epidemiologyCancer geneticsPredictive and prognostic markersMedical infection agents (incl. prions)
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Publications (17)

|May 18, 2026
MLH1 Constitutional Epimutation Screening Requires Highly Sensitive Assays to Identify Lynch Syndrome Patients With Very Low Mosaic Methylation Level.

|May 13, 2026
Follow-up, cancer risk and mortality in Peutz-Jeghers syndrome: Data from the PRED-IdF network.

|Feb 13, 2026
Priority European strategies for sustainable access to high-quality genetic counselling in cancer: A Delphi study.

J Matt McCrary, Els Van Valckenborgh, Denis Horgan

|Jan 29, 2026
Results of a multigene panel testing approach targeting patients with suspected genetic predisposition to pancreatic ductal adenocarcinoma.

Bruno Buecher, Mathilde Warcoin, Emilie Rolland

|Oct 03, 2025
Myeloid neoplasms risks for germline DDX41 pathogenic variants carriers.

Marie-Charlotte Villy, Youenn Drouet, Lise Larcher

|Sep 25, 2025
Hereditary diffuse gastric cancer spectrum associated with germline CTNNA1 loss of function revealed by clinical and molecular data from 351 carrier families and over 37 000 non-carrier controls.

Silvana Lobo, Alexandre Dias, Ana Maria Pedro

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Frequent Collaborators

6 joint publications

Dominique Stoppa-Lyonnet

5 joint publications

Lisa Golmard

4 joint publications

Patrick R Benusiglio

3 joint publications

Bruno Buecher